• Environmental Sciences Bulletin of The Korean Environmental Sciences Society
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• 제4권1호
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• pp.31-42
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• 2000

The dry deposition velocities and fluxes of air pollutants such as SO2(g), O3(g), HNO3(g), sub-micron particulates, NO3(s), and SO42-(s) were estimated according to local meteorological elements in the atmospheric boundary layer. The model used for these calculations was the multiple layer resistance model developed by Hicks et al.1). The meteorological data were recorded on an hourly basis from July, 1990 to June, 1991 at the Austin Cary forest site, near Gainesville FL. Weekly integrated samples of ambient dry deposition species were collected at the site using triple-fiter packs. For the study period, the annual average dry deposition velocities at this site were estimated as 0.87$\pm$0.07 cm/s for SO2(g), 0.65$\pm$0.11 cm/s for O3(g), 1.20$\pm$0.14cm/s for HNO3(g), 0.0045$\pm$0.0006 cm/s for sub-micron particulates, and 0.089$\pm$0.014 cm/s for NO3-(s) and SO42-(s). The trends observed in the daily mean deposition velocities were largely seasonal, indicated by larger deposition velocities for the summer season and smaller deposition velocities for the winter season. The monthly and weekly averaged values for the deposition velocities did not show large differences over the year yet did show a tendency of increased deposition velocities in the summer and decreased values in the winter. The annual mean concentrations of the air pollutants obtained by the triple filter pack every 7 days were 3.63$\pm$1.92 $\mu\textrm{g}$/m3 for SO42-, 2.00$\pm$1.22 $\mu\textrm{g}$/m-3 for SO2, 1.30$\pm$0.59 $\mu\textrm{g}$/m-3 for HNO3, and 0.704$\pm$0.419 $\mu\textrm{g}$/m3 for NO3-, respectively. The air pollutant with the largest deposition flux was SO2 followed by HNO3, SO42-(S), and NO3-(S) in order of their magnitude. The sulfur dioxide and NO3- deposition fluxes were higher in the winter than in the summer, and the nitric acid and sulfate deposition fluxes were high during the spring and summer.

• Asian Journal of Atmospheric Environment
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• 제6권4호
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• pp.246-258
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• 2012

Particulate matter deposited on leaf surfaces may cause erosion/abrasion of epicuticular wax and the malfunction of stomata. However, the deposition processes of particulate matter, such as elemental carbon (EC), has not been studied sufficiently in Asian forest ecosystems. Deposition processes for particulate ${SO_4}^{2-}$ and EC were studied in a Japanese cedar forest in Kajikawa, Niigata Prefecture, Japan, and in a dry evergreen forest and a dry deciduous forest in Sakaerat, Nakhon Ratchasima province, Thailand. The ${SO_4}^{2-}$ fluxes attributed to rainfall outside the forest canopy (RF), throughfall (TF), and stemflow (SF) showed distinct seasonalities at both sites, increasing from November to February at the Kajikawa site and in March/April at the Sakaerat site. Seasonal west/northwest winds in winter may transport sulfur compounds across the Sea of Japan to the Kajikawa site. At the Sakaerat site, pollutants suspended in the air or dry deposits from the dry season might have been washed away by the first precipitations of the wet season. The EC fluxes from RF and TF showed similar variations by season at the Kajikawa site, while the flux from TF was frequently lower than that from RF at the Sakaerat site. Particulate matter strongly adsorbed onto leaf surfaces is not washed away by rainfall and contributes to the EC flux. At the Kajikawa site, Japanese cedar leaf surfaces accumulated the highest levels of particulate matter and could not be neglected when calculating the total flux. When such leaf-surface particles were considered, the contribution of dry deposition to the total EC flux was estimated to be 67%, 77%, and 82% at the Kajikawa site, and at the evergreen and deciduous forests of the Sakaerat site, respectively. Leaf-surface particles must be included when evaluating the dry and total fluxes of particulate matter, in particular for water-insoluble constituents such as EC.

• 환경영향평가
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• 제8권1호
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• pp.1-16
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• 1999

The acid deposition and photochemical modeling study was performed on the Eastern Asia using Regional Acid Deposition Model(RADM). The results of this study show that horizontal distribution of $SO_2$, concentration and dry deposition flux was higher in Beking, Shanghai and central part of Korea. However distribution pattern of sulfate and $O_3$ concentration calculated by RADM were not similar to emission pattern. In daytime, $SO_2$, sulfate and $O_3$ were mixed to whole PBL but in nighttime because of inversion layer these pollutants were suppressed to lower level.

• 한국환경과학회지
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• 제13권5호
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• pp.469-478
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• 2004

Atmospheric bulk (wet and dry) samples were monthly collected in an urban environment (Daeyeon-dong) of Busan over a year, to assess the deposition flux and seasonality of dioxin-like polychlorinated biphenyls (DLPCBs) using stainless steel pots. Deposition fluxes of DLPCBs in bulk samples were determined using high resolution gas chromatography coupled to high resolution mass spectrometry (HRGC/HRMS). Particle deposition fluxes in the urban environment varied from 23 to 98 $mg^2$/year (mean 41 $gm^2$/year). DLPCB deposition fluxes in atmospheric bulk samples ranged from 0.09 to 0.77 ng-$TEQ/m^2$/year (mean 0.35 ng-$TEQ/m^2$/year). Seasonal atmospheric deposition fluxes of DLPCBs were high in winter and low in summer. Atmospheric deposition fluxes of particles and DLPCBs in this study were comparable to or slightly lower values than those of different locations in the world. Monthly DLPCB profiles in deposition bulk samples were similar over a year. Non-ortho PCBs were higher contributions to the total DLPCBs fluxes than mono-ortho PCBs. In particular, PCB 126 had the highest concentrartion (>75%) in all deposition samples, followed by PCB 169 and PCB 156. A highly positive correlation was found among the deposition fluxes of DLPCB species, suggesting the possibility of that the DLPCB contamination originated from one source. The deposition fluxes of DLPCBs were not significantly correlated with temperature and the amount of precipitation even though the summer season with the highest temperature and the largest amount of precipitation showed the lowest DLPCB deposition flux.

• 한국대기환경학회지
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• 제22권4호
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• pp.477-486
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• 2006

Dry deposition fluxes for $SO_2$, particulate sulfate, nitrate, ammonium and $HNO_3$ were estimated in urban area for the time period January$\sim$ October 2005. Fluxes were generated using atmospheric concentration data collected both in Acid Deposition and Air Quality Monitoring Networks, and deposition velocities computed by combining land-use data with meteorological information. The resulting annually averaged $SO_2$, $NO_3$, and aerosol deposition velocities were found to be 0.4 cm/s, 4.3 cm/s and 0.1 cm/s, respectively, and thus deposition rates were 4.4 mg/$m^2$. day for $SO_2$, and 5.4 mg/$m^2$ . day for $NHO_3$, and particulate sulfate, ammonium and nitrate recorded 1.0 mg/$m^2$ . day, 0.4 mg/$m^2$ . day and 0.4 mg/$m^2$ day, respectively. Maximum for in seasonal variation of monthly averaged deposition velocities occurred in summer in contrast to $HNO_3$ showing peak in spring. There was no significant variation for aerosol. The dry to total (wet and dry) deposition contributed about 40% for sulfur and 28% for nitrogen species in this study.

• Environmental Engineering Research
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• 제12권3호
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• pp.118-127
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• 2007

Between June and November 2002, the atmospheric concentrations and dry deposition fluxes of polycyclic aromatic hydrocarbons (PAHs) in Chonju were measured four times each over five days. The total concentration of PAHs in ambient air was $84\;ng/m^3$, with about 90% existing in the vapor phase. Plots of log ($K_p$) vs. log (${P_L}^0$) indicated that PAHs partitioning was not in equilibrium and the particulate characteristics did not change with seasonal variations. The PAHs fluxes to a water surface sampler (WSS) and a dry deposition plate (DDP) were about 14.15 and $1.92\;{\mu}g/m^2/d$, respectively. The flux of the gaseous phase, acquired by subtracting the DDP from the WSS results, was about $12.23\;{\mu}g/m^2/d$. A considerable correlation was shown between the atmospheric concentrations and deposition fluxes in the gaseous phase, but not in the particulate phase, as the fluxes of the particulate phase were dependent on the physical velocity differences of the particulates based on the particle diameter.

• 대한환경공학회지
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• 제22권4호
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• pp.775-784
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• 2000

본 연구는 그리스 대체표면을 사용한 건식침적판(knife-leading-edge surrogate surface)과 물표면 채취기(water surface sampler)를 이용하여 질산염(입자상, 가스상)의 전식침적량을 직접 측정하였다. 평균 가스상 건식침적량($8.3mg/m^2/day$) 이 입자상 건식침적량($3.0mg/m^2/day$)에 비해 훨씬 큰 값을 나타내었다. 직접 측정한 질산염의 가스상 건식침적량과 대기 중 질산($HNO_3$) 농도 사이의 선형회귀분석을 통하여 질산의 가스상 질량전달계수률 구하였다. 이와 같이 구한 질산의 질량전달계수는 이산화황($SO_2$)의 질량전달계수의 약 2배가 되는 값을 보여주었다. 특히, 오존주의보시에는 Graham의 확산법칙을 사용하여 이산화황의 질량전달계수로부터 계산한 질산의 질량전달계수와 대기 중 질산 농도와의 곱으로 추정된 질산염의 가스상 건식침적량에 비해, 측정된 건식침적량이 훨씬 높은 값을 나타내는 특이한 현상을 보였다. 이 결과는 질산 외의 가스상 화학종이 질소산화물의 가스상 건식침적량에 영향을 미친다는 사실을 나타내고 있다. 이론적인 계산결과에 의하면 아질산($HNO_2$) 과 PAN이 질소산화물의 가스상 건식침적량에 기여할 가능성이 높은 것으로 나타났다.

• 한국대기환경학회:학술대회논문집
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• 한국대기환경학회 2001년도 추계학술대회 논문집
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• pp.87-88
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• 2001

대기오염물질 제거에 중요한 역할을 하는 침적 현상은 크게 건성침적(dry deposition)과 습성침적(wet deposition)으로 구분된다. 건성침적은 오염물질이 중력이나 분자 확산에 의해 지면이나 그 부근에 침강ㆍ흡착하는 현상이며, 습성침적은 구름 속의 에어로졸이 응결핵으로 제거되는 성우제거(rainout)와 구름 이하의 고도에서 강수에 의해 제거되는 세척제거(washout)와 같은 현상을 일컫는다. 습성침적은 강수 및 구름 물리와 관련하여 대기 중 오염물질 제거에 큰 비중을 차지함에도 불구하고 건성침적에 비해 그 연구가 미흡한 실정이며, 침적 모형을 이용한 연구는 더욱 찾아보기 어렵다. (중략)

• 대한환경공학회지
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• 제22권3호
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• pp.575-585
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• 2000

서울지역의 질량 및 중금속 건식침적량과 대기중 입자의 입경분포를 1998년 7월부터 11월까지 건식침적판, 다단계 관성충돌 채취기(Cascade Impactor) 및 조대업자 채취기(Coarse Particle Sampler)를 사용하여 측정하였다. 인위적 오염원에 기인한 중금속(Cu, Mn, Ni, Pt, Zn)의 건식침적량이 주로 자연적 오염원에 기인한 중금속(Al, Ca)의 건식침적량에 비하여 약 10배에서 100배 정도 낮은 값을 나타내었다. 완전한 총 입자 및 중금속 입자의 입경분포는 입자 입경이 $10{\mu}m$보다 작은 영역에서 두 개의 peak를 보이고 $10{\mu}m$보다 큰 입자 영역에서 또다른 peak을 보이는 삼봉형(trimodal) 입경분포를 보여주었다. Sehmel-Hodgson 모델을 사용하여 건식침적속도를 추정하고 이를 이용하여 총 입자 및 중금속 입자의 건식침적량을 계산하기 위하여 다단계 모델(Multi-step model)을 사용하였다. 이 방법에 의하면, 건식침적량은 입자의 입경이 $10{\mu}m$보다 큰 입자들의 높은 건식침적속도에 의하여 크게 영향을 받고 이로부터 건식침적은 $10{\mu}m$보다 큰 입자들의 침적이 대부분을 차지한다는 것을 보여주었다. 측정된 입자의 입경분포와 추정된 건식침적속도를 이용하여 다단계 모델을 통하여 예측된 건식침적량은 직접 측정된 건식침적량과 비교하였을 때 잘 일치하였다.

• 한국대기환경학회:학술대회논문집
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• 한국대기환경학회 2000년도 추계학술대회 논문집
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• pp.109-111
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• 2000

지금까지 대기침적량의 산정에는 크게 대기중의 오염물질 농도와 침적속도를 이용하여 추정하는 방법 (atmospheric flux methods)과 대리표면을 이용하여 건성침적량을 직접 측정하는 표면분석 방법(surface analysis methods)이 주로 이용되고 있다. 전자는 대기중 오염물질 농도를 관측ㆍ분석함으로써 eddy correlation, aerodynamic gradient methods 등의 미기상학적인 방법이 여기에 해당되며 균일하지 못한 표면이나 중력침강이 주가되는 조대입자에 대해 사용이 제한되는 단점이 있다. 이에 반해 대체표면을 사용하는 방법은 일반적으로 시료채취 및 분석과정에 있어서 통제가 용이하기 때문에 현재 광범위하게 널리 사용되고 있다. (중략)